GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ1 in Dinoroseobacter shibae DFL-12

Align 3-oxoadipyl-CoA thiolase; EC 2.3.1.174 (characterized, see rationale)
to candidate 3606642 Dshi_0074 acetyl-CoA acetyltransferase (RefSeq)

Query= uniprot:D8ITH5
         (401 letters)



>FitnessBrowser__Dino:3606642
          Length = 392

 Score =  254 bits (648), Expect = 4e-72
 Identities = 159/398 (39%), Positives = 230/398 (57%), Gaps = 15/398 (3%)

Query: 5   ICDAIRTPFGRYGGALGAVRADDLAAAPIRSLMERNPGVDWSRVEDILYGCANQAGEDNR 64
           IC A RTP G + G    V A  L  A I   +  + GV  ++V ++L GC   AG+  +
Sbjct: 6   ICGAARTPMGGFQGVFSDVSAAQLGGAAIAGALA-DAGVAPAQVNELLMGCVLPAGQ-GQ 63

Query: 65  NVARMAGLLAGLPIAVPGSTVNRLCGSSLDAVGMAARAIKSGEVQLMIAGGVESMTRAPF 124
             AR AG  AGL  AVP +T+N++CGS + A  +A   I  G+  L++AGG+ESMT AP+
Sbjct: 64  APARQAGYAAGLGDAVPATTLNKMCGSGMKAAMIACDQIALGQSDLVVAGGMESMTNAPY 123

Query: 125 VMGKAESAFARSAAIFDTTIGWRFVNPLMKAQYGIDSMPETAENVATDFQINRADQDAFA 184
           ++ K     AR        I   F++ L  A      M   AE+ A  FQ  RA QD +A
Sbjct: 124 LLDKMRGG-ARIG--HGQVIDHMFLDGLEDAYDKGRLMGTFAEDCAEAFQFTRAAQDTYA 180

Query: 185 LRSQQRWAAAQAAGFFAGEIAPLTIPQKKGDPLVVTTDEHP---RPDTTLATLAKLKGVV 241
           L S +   AA+A+  FA E+ P+T+  +KG+ +V+  DE P   RP+     +  LK   
Sbjct: 181 LGSLENALAAEASEAFAMELVPVTVSGRKGETVVIR-DEQPAAARPEK----IPHLKPAF 235

Query: 242 RPDGTVTAGNASGVNDGACALLLASPKAADLYRLKPRARVLGMATAGVAPRIMGFGPAPA 301
           R DGTVTA N+S ++DGA AL+LA    A+ + L  RARVLG A+    P +    P PA
Sbjct: 236 RKDGTVTAANSSSISDGAAALVLADAGQAEAHGLPVRARVLGHASHAQKPALFPTAPVPA 295

Query: 302 VRKVLAQVGLTLAQMDVIELNEAFAAQGLAVMRDLGLPDDAAHVNPNGGAIAIGHPLGAS 361
            RK+L ++G  +A +D+ E+NEAFA   +A M ++G+P +   +N NGGA A+GHP+GAS
Sbjct: 296 ARKLLDRLGWCVADVDLWEVNEAFAVVPMAFMHEMGVPRE--KMNVNGGACALGHPIGAS 353

Query: 362 GARLVTTAINQLERSGGRYALCTMCIGVGQGIALVIER 399
           GAR++ T +N +E    +  +  +CIG G+G A+ +ER
Sbjct: 354 GARILVTLLNAMEARDLKRGVAAICIGGGEGTAIALER 391


Lambda     K      H
   0.320    0.135    0.394 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 402
Number of extensions: 19
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 401
Length of database: 392
Length adjustment: 31
Effective length of query: 370
Effective length of database: 361
Effective search space:   133570
Effective search space used:   133570
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory